mild hearing impairment Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of a mild form of hearing impairment. (Human Phenotype Ontology, HP_0012712)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012712
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Genes

2 genes associated with the mild hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
MARS2 methionyl-tRNA synthetase 2, mitochondrial
MFN2 mitofusin 2